103 related articles for article (PubMed ID: 16319722)
1. Unique tauopathy in Fukuyama-type congenital muscular dystrophy.
Saito Y; Motoyoshi Y; Kashima T; Izumiyama-Shimomura N; Toda T; Nakano I; Hasegawa M; Murayama S
J Neuropathol Exp Neurol; 2005 Dec; 64(12):1118-26. PubMed ID: 16319722
[TBL] [Abstract][Full Text] [Related]
2. Breached cerebral glia limitans-basal lamina complex in Fukuyama-type congenital muscular dystrophy.
Saito Y; Murayama S; Kawai M; Nakano I
Acta Neuropathol; 1999 Oct; 98(4):330-6. PubMed ID: 10502035
[TBL] [Abstract][Full Text] [Related]
3. Fukutin protein is expressed in neurons of the normal developing human brain but is reduced in Fukuyama-type congenital muscular dystrophy brain.
Saito Y; Mizuguchi M; Oka A; Takashima S
Ann Neurol; 2000 Jun; 47(6):756-64. PubMed ID: 10852541
[TBL] [Abstract][Full Text] [Related]
4. Altered glycosylation of alpha-dystroglycan in neurons of Fukuyama congenital muscular dystrophy brains.
Saito Y; Yamamoto T; Mizuguchi M; Kobayashi M; Saito K; Ohno K; Osawa M
Brain Res; 2006 Feb; 1075(1):223-8. PubMed ID: 16466646
[TBL] [Abstract][Full Text] [Related]
5. Are breaches in the glia limitans the primary cause of the micropolygyria in Fukuyama-type congenital muscular dystrophy (FCMD)? Pathological study of the cerebral cortex of an FCMD fetus.
Nakano I; Funahashi M; Takada K; Toda T
Acta Neuropathol; 1996; 91(3):313-21. PubMed ID: 8834545
[TBL] [Abstract][Full Text] [Related]
6. Tau-positive fine granules in the cerebral white matter: a novel finding among the tauopathies exclusive to parkinsonism-dementia complex of Guam.
Yamazaki M; Hasegawa M; Mori O; Murayama S; Tsuchiya K; Ikeda K; Chen KM; Katayama Y; Oyanagi K
J Neuropathol Exp Neurol; 2005 Oct; 64(10):839-46. PubMed ID: 16215455
[TBL] [Abstract][Full Text] [Related]
7. Oxidative stress in the brain of Fukuyama type congenital muscular dystrophy: immunohistochemical study on astrocytes.
Yamamoto T; Shibata N; Kobayashi M; Saito K; Osawa M
J Child Neurol; 2002 Nov; 17(11):793-9. PubMed ID: 12585716
[TBL] [Abstract][Full Text] [Related]
8. Characteristics of neurons and glia in the brain of Fukuyama type congenital muscular dystrophy.
Yamamoto T; Kato Y; Kawaguchi-Niida M; Shibata N; Osawa M; Saito K; Kröger S; Kobayashi M
Acta Myol; 2008 Jul; 27(1):9-13. PubMed ID: 19108571
[TBL] [Abstract][Full Text] [Related]
9. Fukutin expression in glial cells and neurons: implication in the brain lesions of Fukuyama congenital muscular dystrophy.
Yamamoto T; Kato Y; Karita M; Takeiri H; Muramatsu F; Kobayashi M; Saito K; Osawa M
Acta Neuropathol; 2002 Sep; 104(3):217-24. PubMed ID: 12172906
[TBL] [Abstract][Full Text] [Related]
10. Immature astrocytes in Fukuyama congenital muscular dystrophy: an immunohistochemical study.
Yamamoto T; Armstrong D; Shibata N; Kanazawa M; Kobayashi M
Pediatr Neurol; 1999 Jan; 20(1):31-7. PubMed ID: 10029257
[TBL] [Abstract][Full Text] [Related]
11. Cerebellar micropolygyria in Fukuyama congenital muscular dystrophy: observations in fetal and pediatric cases.
Takada K; Nakamura H
Brain Dev; 1990; 12(6):774-8. PubMed ID: 2092587
[TBL] [Abstract][Full Text] [Related]
12. Cortical dysplasia in congenital muscular dystrophy with central nervous system involvement (Fukuyama type).
Takada K; Nakamura H; Tanaka J
J Neuropathol Exp Neurol; 1984 Jul; 43(4):395-407. PubMed ID: 6737009
[TBL] [Abstract][Full Text] [Related]
13. Cortical dysplasia in a 23-week fetus with Fukuyama congenital muscular dystrophy (FCMD).
Takada K; Nakamura H; Suzumori K; Ishikawa T; Sugiyama N
Acta Neuropathol; 1987; 74(3):300-6. PubMed ID: 3314312
[TBL] [Abstract][Full Text] [Related]
14. Pial-glial barrier abnormalities in fetuses with Fukuyama congenital muscular dystrophy.
Yamamoto T; Toyoda C; Kobayashi M; Kondo E; Saito K; Osawa M
Brain Dev; 1997 Jan; 19(1):35-42. PubMed ID: 9071488
[TBL] [Abstract][Full Text] [Related]
15. Cortical dysplasia in Fukuyama congenital muscular dystrophy (FCMD): a Golgi and angioarchitectonic analysis.
Takada K; Nakamura H; Takashima S
Acta Neuropathol; 1988; 76(2):170-8. PubMed ID: 2457291
[TBL] [Abstract][Full Text] [Related]
16. Sporadic Pick's disease: a tauopathy characterized by a spectrum of pathological tau isoforms in gray and white matter.
Zhukareva V; Mann D; Pickering-Brown S; Uryu K; Shuck T; Shah K; Grossman M; Miller BL; Hulette CM; Feinstein SC; Trojanowski JQ; Lee VM
Ann Neurol; 2002 Jun; 51(6):730-9. PubMed ID: 12112079
[TBL] [Abstract][Full Text] [Related]
17. [Fukuyama-type congenital muscular dystrophy].
Toda T
Rinsho Shinkeigaku; 2000 Dec; 40(12):1297-9. PubMed ID: 11464484
[TBL] [Abstract][Full Text] [Related]
18. Vascular alterations in Fukuyama type congenital muscular dystrophy.
Sugino S; Miyatake M; Ohtani Y; Yoshioka K; Miike T; Uchino M
Brain Dev; 1991; 13(2):77-81. PubMed ID: 1892223
[TBL] [Abstract][Full Text] [Related]
19. Clinicopathological study on eyes from cases of Fukuyama type congenital muscular dystrophy.
Hino N; Kobayashi M; Shibata N; Yamamoto T; Saito K; Osawa M
Brain Dev; 2001 Mar; 23(2):97-107. PubMed ID: 11248458
[TBL] [Abstract][Full Text] [Related]
20. Congenital muscular dystrophy with characteristic radiological findings similar to those with Fukuyama congenital muscular dystrophy.
Garg A; Gulati S; Gupta V; Kalra V
Neurol India; 2004 Dec; 52(4):496-8. PubMed ID: 15626844
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
